SCN4B Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2731494

Produktdetails

Target: SCN4B (Sodium Channel, Voltage-Gated, Type IV, beta Subunit (SCN4B))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses SCN4B Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human SCN4B (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: SCN4B (Sodium Channel, Voltage-Gated, Type IV, beta Subunit (SCN4B))

Andere Bezeichnung: Scn4b (SCN4B Produkte)

Synonyme: LQT10 Protein, Navbeta4 Protein, Gm1471 Protein, sb:cb973 Protein, scn4b.2 Protein, si:ch211-139a5.5 Protein, scn4b.1 Protein, scn4b1 Protein, zgc:165389 Protein, sodium voltage-gated channel beta subunit 4 Protein, sodium channel, type IV, beta Protein, sodium channel, voltage-gated, type IV, beta b Protein, sodium channel, voltage-gated, type IV, beta a Protein, SCN4B Protein, Scn4b Protein, scn4bb Protein, scn4ba Protein

Hintergrund: The protein encoded by this gene is one of several sodium channel beta subunits. These subunits interact with voltage-gated alpha subunits to change sodium channel kinetics. The encoded transmembrane protein forms interchain disulfide bonds with SCN2A. Defects in this gene are a cause of long QT syndrome type 10 (LQT10). Three protein-coding and one non-coding transcript variant have been found for this gene.[provided by RefSeq, Mar 2009].

Molekulargewicht: 22 kDa

NCBI Accession: NP_777594